A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081535



Internal ID21465817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69171080..69171129hg38UCSC Ensembl
chr15:69463419..69463468hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586455
Supporting Variants
SamplesHG03065
Known GenesGLCE, MIR548H4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081535
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer